Canonical Allele Identifier: PA2825067511
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 641699
ClinVar RCV Id: RCV000794999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Ser309Arg
CA859083
NM_000098.3:c.927T>A
CA340394134
NM_000098.3:c.925A>C
CA340394140
NM_000098.3:c.927T>G